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We are opportunity and talent—a company specializing in engineering services, offering design, project engineering, outsourcing, and training.\n \n \n\nWe are seeking an Electrical Engineer to work in Alcobendas for a company providing packaging services to the pharmaceutical sector.\n \n \n\nThe main responsibilities will include panel layout, single-line diagram drafting, cable sizing calculations, bill of materials preparation, and technical specifications for low-voltage (LV) and medium-voltage (MV) projects.\n \n \n\n**Requirements:** \n\n* Education: Degree in Electrical Engineering or related field.\n* Proven experience in the responsibilities described above.\n* Proficiency with tools such as NEPLAN, ETAP, and DigSILENT.\n* Technical English.\n\n\n**Conditions:** \n\n* Work for a rapidly growing company with multidisciplinary and highly qualified teams.\n* Opportunities for professional development and continuous improvement—we are expanding across all departments.\n* Committed to our employees’ well-being.\n* Close-knit team, positive working environment, and strong camaraderie.\n\n\nJoin our team! 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At **Ferrovial**, we are not just a company; we are a community of innovators and trailblazers. Listed on three major stock markets: Nasdaq (US), Euronext Amsterdam (Netherlands) and IBEX 35 (Spain), we are also member of the Dow Jones Sustainability Index and FTSE4Good. We operate in more than 15 countries and have a workforce of over 24,000 professionals worldwide. Ferrovial’s activity is carried out through our business units, including Highways, Airports, Construction, and Energy.\n\n\nOur **Corporate** organization oversees business activities, providing strategic planning, communication, legal, finance and human resources services to the business units. 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This role contributes to advancing Ferrovial’s commitment to climate action, natural capital preservation, circular economy, and water resource management. 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Move the world together!** Innovative, creative, respectful, and diverse are some of the ways we describe ourselves. We are motivated by challenges, and we collaborate across our business units to move the world together. Your journey to a fulfilling career starts here!\n\n\nFerrovial is an equal opportunity employer. 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Our Patient and Site Centric Solutions (PSCS) team partners with experts across the business to design strategies that help sponsors enroll and retain the right patients — while ensuring sites feel supported and empowered every step of the way.\nIf you are passionate about improving the patient experience in research and want to influence global trial performance, this role offers a unique opportunity to make meaningful impact.**What you will do*** Develop and implement best‑in‑class patient recruitment, retention, and site‑engagement strategies to support customer enrollment goals.\n* Partner cross‑functionally to shape PSCS strategy both pre‑ and post‑award.\n* Lead elements of solution innovation to enhance our global recruitment and retention offerings.\n* Present strategy recommendations and insights during client bid‑defense meetings.\n* Create data‑driven budget estimates for proposed solutions.\n* Represent IQVIA at industry events, conferences, or webinars as a thought leader.\n* Collaborate with internal stakeholders to ensure all solutions meet quality and regulatory standards.\n* Mentor and coach team members to support development and team excellence.\n* Drive process improvement initiatives within PSCS.\n* Serve as a trusted liaison for internal teams and clients on recruitment strategy topics.\n\n**What you need to succeed*** Bachelor’s degree required.\n* 10\\+ years of relevant experience, including 5\\+ years in leadership roles.\n* Strong understanding of clinical development, patient recruitment, and site engagement.\n* In‑depth knowledge of GCP/ICH and applicable regulatory guidelines.\n* Demonstrated ability to analyze data and translate insights into effective strategies.\n* Solid understanding of clinical research financial parameters and budget management.\n* Excellent communication and presentation skills with the ability to influence stakeholders.\n* Strong leadership capabilities with a collaborative, relationship‑oriented style.\n* Proficiency in Microsoft PowerPoint, Excel, and Word.\n* Strong organizational and problem‑solving skills with the ability to manage competing priorities.\n\n**Why join IQVIA**\nAt IQVIA, you’ll be part of a global team driving smarter healthcare for everyone, everywhere. You’ll work alongside innovators, clinicians, analysts, and strategists who are committed to improving patient outcomes and shaping the future of clinical development. \n\nExpect a culture built on collaboration, continuous learning, and opportunities for growth — supported by tools and insights that help you do your best work.\nIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.\nAt IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. 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Mayor, nº 1, 28100 Alcobendas, Madrid, Spain","infoId":"6510607348454712","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Revenue Financial Controller - Laboratorio Central Health Diagnostics Quirónsalud (Alcobendas)","content":"**At Quirónsalud, your career has a purpose.**\n\n\n\nAt **Quirónsalud**, we do not just lead the healthcare sector; we are **transforming** it. With state-of-the-art technology and a network of over **58 hospitals in Spain and more than 180 healthcare centres across Europe**, backed by **Fresenius-Helios**, we work with a clear mission: **improving lives**.\n\n\n\nWe are looking for professionals who want to **grow, innovate and be part of a team where excellence is part of everyday life.**\n\n\n**Join our team**\n\n\n**Position:** Revenue Financial Controller \n\n**Location:** Laboratorio Central Health Diagnostics (Alcobendas)\n\n\n**Key responsibilities:**\n\n\n* Lead the preparation of the annual revenue + activity budget and monitor its execution.\n* Monitor contracts and ensure correct tariff application.\n* Participate in defining and improving revenue and activity dashboards (KPIs_Power BI).\n* Contribute ideas and innovation to improve existing processes and systems.\n* Perform revenue closing and reconciliation with various profit centres and business units.\n* Prepare monthly and annual closing reports on revenue figures (billing/provisions/activity/KPIs).\n* Monitor monthly performance versus prior year and budget, analyse variances and propose improvements.\n* Monitor and evaluate profitability.\n* Analyse balance sheet accounts (revenue, bad debts).\n* Support audits.\n\n**What we offer:**\n\n\n* **Immediate onboarding** into a collaborative and specialised team.\n* **Attractive, competitive and market-aligned remuneration package.**\n* **An environment that fosters your development**\n* You will benefit from the support of an experienced team that will help you strengthen your skills and advance your career.\n* **Continuous training**: we will stimulate your learning and development through our **Quirónsalud University** and our **specific training plans**, enabling your personal and professional growth.\n\n**We care about your wellbeing**\n\n\n* **Access to our Health and Wellbeing Programme**, including initiatives such as:\n* + **Healthcare:** physical and mental wellbeing programmes (access to medical services, health maintenance programmes, psychological support).\n\t+ **Financial wellbeing:** flexible compensation schemes, salary management facilities and exclusive discounts.\n\t+ **Volunteering programme.**\n\n\nWe’re waiting for you!\n\n\n*At Quirónsalud, we promote integration and respect for diversity. 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The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. \n\nA fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and **develop their career in the research and development of cutting\\-edge therapeutics**. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).\n\n\nResponsibilities :\n* Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager\n* Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy\n* Compile and maintain project\\-specific status reports within the clinical trial management system\n* Interact with the internal project team, Sponsor, study sites, and third\\-party vendors\n* Manage and perform quality control of our internal regulatory filing system\n* Provide oversight and management of study supplies\n* Create and maintain project timelines\n* Coordinate project meetings and produce quality minutes\n\n\nQualifications :\n* PhD in Life Sciences\n* Fluency in English with solid presentation skills\n* Ability to work in a fast\\-paced dynamic industry within an international team\n* Prior experience within the CRO or pharmaceutical industry not required but will be advantageous\n\n\nMedpace Overview :\n\nMedpace is a full\\-service clinical contract research organization (CRO). We provide Phase I\\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\\-viral and anti\\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\\+ countries.\nWhy Medpace? :\n\nPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. \n\nThe work we’ve done over the past 30\\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. 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diagnosis and audit of buildings (new and existing).\n\n· Development of energy efficiency improvement projects.\n\n· Administrative and regulatory follow-up of certifications.\n\n· Collaboration with internal engineers and technicians.\n\n· Participation in construction, rehabilitation, and sustainable renovation projects.\n\n* **Candidate Profile**\n\n· Degree in Architecture or Engineering recognized in Spain.\n\n· Current registration with the Official College of Architects (or equivalent for engineers).\n\n· Legal authorization to prepare and sign EECs.\n\n· Experience in energy audits or sustainable design is valued.\n\n· Knowledge of Spanish energy efficiency regulations (RD 390/2021, etc.).\n\n· Proficiency in energy certification software (CE3X, HULC, etc.).\n\n· French language required.\n\n· Rigor, autonomy, and ability to work as part of a team.\n\n* **Terms**\n\n· Contract: CDD (fixed-term)\n\n· Location: MADRID\n\n· Remuneration: commensurate with profile and experience\n\n· Start date: as soon as possible\n\n* **Applications**\n\nSend CV to: contact@energestia.es\n\nEmployment type: Full-time\n\nWork location: On-site","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768544259488","seoName":"Ingeniero+de+eficiencia+energ%C3%A9tica","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-env-earth-geosciences/ingeniero%2Bde%2Beficiencia%2Benerg%25c3%25a9tica-6509366521459312/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"f619c228-c0dd-4d5a-a5a6-b630c805fe80","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace 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Candidates can be located anywhere within one of the countries listed in the job ad.* *Candidates must have a permanent right to work in a country they apply for.*\nJoin IQVIA’s Sponsor\\-Dedicated FSP team and help advance healthcare through real\\-world evidence. We bring together scientific expertise and real\\-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.**Overview:**\nDesign and conduct epidemiological studies to generate real\\-world evidence within time, budget, and quality standards, including but not limited to natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post\\-authorization studies. 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Master’s degree in Epidemiology plus 7\\-9 years of experience in lieu of PhD may be acceptable.**\n* **Oncology Specific: expert knowledge and extensive experience (at least 2\\+ years leading studies) with cancer epi (solid tumor experience a plus), extensive experience with oncology EMR databases, extensive experience with conducting cancer epi studies.**\n* **Pharmaco Epidemiology Specific: expert knowledge and extensive experience with pharmacoepi methods (i.e., signal detection and validation methods), expert understanding of regulatory requirements for safety reporting and analysis, RMPs, and PASS both US and global.**\n* Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.\n* Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases.\n* A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.\n* Demonstrated ability to function with an increasing level of autonomy and to develop productive cross\\- functional collaborations in a matrix environment.\n* Ability to manage priorities and performance targets.\n\n**What’s in it for you?*** Be part of a forward\\-thinking team that helps shape the next generation of evidence\\-based healthcare.\n* Work hand\\-in\\-hand with one leading sponsor, gaining deep expertise in their therapies.\n* Access IQVIA’s global network who supports your growth.\n\n\nThis is your chance to make an impact, while building a career that matters.\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768541222649","seoName":"senior-epidemiologist-oncology-breast-cancer-rwe-sponsor-dedicated-multiple-locations-home-based","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-laboratory-technical-services/senior-epidemiologist-oncology-breast-cancer-rwe-sponsor-dedicated-multiple-locations-home-based-6509327649920112/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"90c1e88e-8345-4e7d-8c15-4f4b3811f91f","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1768541222649,"categoryName":"Laboratory & Technical Services","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4385","location":"C/ de Juan Esplandiú, 11-13, Retiro, 28007 Madrid, Spain","infoId":"6507121906073912","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Site Contract Analyst - IQVIA Biotech","content":"Madrid, Spain \\| Full time \\| Home\\-based \\| R1512143**Job available in additional locations** **Site Contracts Associate****IQVIA Biotech****Poland, Serbia, Spain, Slovakia \\- Homebased**\nIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.**Job Overview**\nSupport the delivery of all required start\\-up contracting activities for selected sponsors, studies or multi\\-protocol programs as determined by either the agreed algorithm or the Sponsor’s requirements, including pre\\-award activities.**Essential Functions*** Develop simple investigator grant estimates and proposal text to support the proposal development process.\n* Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi\\-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.\n* Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.\n* Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.\n* Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.\n* Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.\n* Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.\n* Comply with contract management and quality standards. Provide administrative and operational support to investigator site contract analysts, managers and directors as required.\n* Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.\n\n**Qualifications and Skills*** Bachelor's Degree in life sciences or health care\n* 2 \\- 5 years relevant experience, including demonstrable experience acting as a contract negotiator.\n* Relevant sponsor or clinical research organization clinical site contracting experience.\n* Good negotiating and communication skills.\n* Good interpersonal skills and a strong team player.\n* Strong technical writing skills.\n* Understanding of regulated clinical trial environment and knowledge of drug development process.\n* Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.\n* Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards.\n* Good organizational and planning skills.\n* Strong knowledge of Microsoft Office and e\\-mail applications.\n* Ability to interpret pricing models and to prepare proposals, bid grids and budgets.\n* Good understanding of clinical trial contract management.\n* Ability to establish and maintain effective working relationships with co\\-workers, managers and sponsors.\n\n\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com\nThe potential base pay range for this role, when annualized, is zł102,800\\.00 \\- zł272,500\\.00\\. The actual base pay offered may vary based on a number of factors including job\\-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part\\-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.","price":"€ 102,800-272,500/year","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768368898912","seoName":"site-contract-analyst-iqvia-biotech","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-other3/site-contract-analyst-iqvia-biotech-6507121906073912/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"62cd49be-7014-4e20-8f71-635c37a8a0b0","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1768368898912,"categoryName":"Other","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4375","location":"C. de Santiago, 22, 28801 Alcalá de Henares, Madrid, Spain","infoId":"6506003121600112","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Cook/Cook - Residential Center DomusVi Alcalá de Henares","content":"**Description:**\n----------------\n\n\nAt DomusVi, caring means **sharing humanity**, growing as a professional, and being part of work that transcends everyday life.\n\n\n\nWe are looking for professionals who wish to practice their vocation in an environment where empathy, innovation, and respect are part of every working day.\n\n\n**Why DomusVi?**\n\n\nBecause we are the largest network of socio-healthcare centers and services in Spain, with over **28,000 committed professionals**.\n\n\n\nWe operate from a close, professional, and human perspective, where each user, employee, and family member matters.\n\n\n**Our values define us:**\n\n \n\n* **The art of caring:** We apply knowledge and humanity to care and well-being.\n* **Pioneering spirit:** Innovation and technology are part of our daily routine.\n* **Innate empathy:** We value active and empathetic listening.\n* **Shared trust:** We foster relationships based on commitment and mutual trust.\n* **Emotional sincerity:** We bring authenticity to every relationship.\n\n**What you’ll find at DomusVi**\n\n \n\n* A culture centered on caring for and respecting people (users, employees, families).\n* An interdisciplinary and collaborative team that supports you, listens to you, and helps you develop.\n* Job stability and conditions adapted to your needs.\n* Time to devote to what matters most: high-quality care.\n* Spaces to develop and grow professionally.\n\n**What will you do as a cook?**\n\n* Support and assist the Head Chef and/or Kitchen Manager.\n* Receive orders: control products upon receipt, verify raw materials.\n* Prepare menus following the Technical Sheets for each dish included in the menu.\n* Know and ensure compliance with current regulations regarding food service.\n* Ensure the established service is delivered to maximize user satisfaction.\n* Access and use the DOMUSCHEF tool to: generate daily production reports and place orders for raw materials needed to prepare menus (in the absence of the Kitchen Manager/Head Chef).\n\n**What we offer:**\n\n \n\n* **Contract: temporary, 3 to 6 months, with conversion to permanent contract**\n* **Working hours: 89%**\n* **Shifts: rotating, 08:30–15:00 / 15:30–21:30**\n* **Start date:** immediate\n* **Work environment:** collaborative and respectful\n* **Work-life balance**\n* **Continuous training, Social Benefits, and Professional Development:** enabling you to grow within a company in constant evolution.\n\n \n\n\n**Requirements:**\n---------------\n\n \n\n \n\n* Candidate with training in Hospitality and Catering and at least 12 months’ experience in a similar position, preferably in Collective Catering.\n* Positive consideration will be given to candidates holding Food Handler certification and training on the safe use of cleaning chemicals.\n* Positive consideration will be given to candidates holding additional training related to the field, as well as complementary training promoting Equality.\n\n**Would you like to work somewhere your vocation and professional development go hand in hand?**\n\n\nAt DomusVi, **we share humanity**, caring for both those we serve and those who form part of our team.\n\n\n**We look forward to welcoming you!**","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768281493875","seoName":"cook-residential-center-domusvi-alcala-de-henares","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-bio-biomed-sciences/cook-residential-center-domusvi-alcala-de-henares-6506003121600112/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"fa0bcace-fc68-4dcb-8e3e-b3230f1079de","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Alcalá de Henares,Comunidad de Madrid","unit":null}]},"addDate":1768281493875,"categoryName":"Biological & Biomedical Sciences","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4380","location":"C. Álava, 5, 28500 Arganda del Rey, Madrid, Spain","infoId":"6506003080896112","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Cosmetic Laboratory Quality Control Technician","content":"We are looking for you as:\n\n\n**Cosmetic Laboratory Quality Control Technician**\n=================================================\n\n\n**Location** \n\nMadrid\n\n\n**Contract Type** \n\nTemporary\\+Indefinite\n\n\n**Start Date** \n\nImmediate\n\n\n\nInternational leading company in the cosmetic industry, headquartered in Arganda del Rey. We specialize in the manufacturing and production of skin and hair care products in liquid and wipe formats. We need to hire a person for the Technical and Quality Control area.\n\n\n**Requirements:**\n---------------\n\n\n* Higher Technician in Laboratory Analysis and Quality Control or equivalent\n* Experience in cosmetic laboratories\n* Experience in physicochemical analysis\n\n**Job Description:**\n---------------------------\n\n\n* Raw material, semi-finished product and finished product analysis\n* pH, density, viscosity and refractive index analysis\n* Issuance and transcription of test reports\n* Sampling, analysis and issuance of test reports\n* Conducting attribute-based inspection controls\n\n**What we offer you:**\n---------------------\n\n\n* Development and growth opportunities\n* Salary according to merit\n* Working hours: Monday to Friday, rotating shifts from 06:00 to 14:00 / 14:00 to 22:00 / 22:00 to 06:00\n* Work location: Arganda del Rey.\n\n### **Got more questions?**\n\n\n\nIf you have any doubts, contact us at phone number 91 871 41 50\n\n\n### **Address**\n\n\n\nCalle Álava, 5 \n\n28500 \\- Arganda del Rey","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768281490694","seoName":"technical-quality-control-laboratory-cosmetic","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-laboratory-technical-services/technical-quality-control-laboratory-cosmetic-6506003080896112/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"ebdb7d3b-0f8e-45d8-800a-7ad1dd2ab1ad","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Arganda del Rey,Comunidad de Madrid","unit":null}]},"addDate":1768281490694,"categoryName":"Laboratory & Technical Services","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4385","location":"C/ de Juan Esplandiú, 11-13, Retiro, 28007 Madrid, Spain","infoId":"6505989111961912","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Translation Project Manager, Linguistic Validation & eCOA","content":"Madrid, Spain \\| Full time \\| Home\\-based \\| R1515039**Job available in additional locations** **The Translation Project Manager – Linguistic Validation and eCOA** is responsible for the development and harmonization of the Linguistic Validation and screenshot reviews of Clinical Outcome Assessments (COA) process within the IQVIA Translations team. Including but not limited to, Patient Reported Outcomes, Patient Diaries, Clinician Reported Outcomes, Observer Reported Outcomes and Performance Measures.* Manage multiple Linguistic Validation and eCOA projects at any one time from receipt to completion\n* Liaise with the client to assess and agree project parameters and requirements\n* Coordinate and communicate with interviewers and recruiters for the purpose of conducting debriefing interviews, analyzing results, and making recommendations for improvements.\n* Act as main point of contact for internal/external clients and manage any escalations or issues that may arise\n* Assess clients needs in line with industry Best Practices per request\n* Assess project scope to select appropriate vendors and negotiate deadlines effectively\n* Establish and maintain excellent relationships with freelance, agency and in house linguists globally\n* Monitor and manage the status of assigned projects to effectively anticipate and prevent issues\n* Accurately complete project finances including quoting and budgeting\n* Prepare and maintain project and process documentation and information\n* Understand and adhere to the Quality Management System\n* Comply with relevant and applicable IQVIA procedures and SOPs\n* Work with Team Leads to help in the training and development of junior staff\n* Ensure that high quality is maintained for all projects through QA checks\n\n**Requirements:*** 2\\-3 years of experience specializing in Linguistic Validation as a Project Manager in the Language Services industry\n* Bachelor's degree, ideally in a linguistic, business or scientific field\n* Fluency in English is essential, an additional language would be advantageous\n* Excellent written/verbal communication skills\n* Excellent attention to detail to ensure that high quality standards are maintained\n* Ability to meet strict deadlines and to manage competing priorities and changing demands.\n* Excellent problem solving and analytical skills\n* Ability to follow instructions and work independently whilst using own initiative.\n* Demonstration of advanced IT skills\n* Experience working with technical files, TMS and CAT tools, experience working with XTRF and/or memoQ would be highly advantageous\n* Ability to establish and maintain effective working relationships with colleagues, managers and clients\n\n\nIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.\nAt IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\\-talented collaboration harnesses innovation to deliver superior outcomes.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768280399371","seoName":"translation-project-manager-linguistic-validation-and-ecoa","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-other3/translation-project-manager-linguistic-validation-and-ecoa-6505989111961912/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"1e7670a1-ab11-489a-bcde-fac514946bff","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1768280399371,"categoryName":"Other","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4380","location":"C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain","infoId":"6504938132608112","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Clinical Research Physician","content":"Job Summary :\n\nWe are seeking Clinical Research Physicians to join our dynamic team. The Clinical Research Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Clinical Research Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Clinical Research Physicians in the following Therapeutic Areas:\n* Psychiatry\n* Pediatric / Neuromuscular Neurology\n* GI / Hepatology\n* Dermatology\n* Metabolic / Endocrinology\n\n\n\\*\\*All Medical Directors have hybrid WFH flexibility.\nResponsibilities :\n* Provide medical management and expertise for clinical trials;\n* Contribute medical expertise to study reports, regulatory documents, and manuscripts;\n* Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;\n* Participate in new business development through involvement in proposal and sponsor meetings as requested;\n* Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;\n* Follow specific research related protocol and lead others in strict adherence to the policies.\n\n\nQualifications :\n* Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred;\n* Must have prior clinical trial research experience; and\n* Previous experience in pharmaceutical\\-related clinical research is preferred.\n\n**Travel**: up to 20%\nMedpace Overview :\n\nMedpace is a full\\-service clinical contract research organization (CRO). We provide Phase I\\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\\-viral and anti\\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\\+ countries.\nWhy Medpace? :\n\nPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. \n\nThe work we’ve done over the past 30\\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks**\n\n* Flexible work environment\n* Competitive compensation and benefits package\n* Competitive PTO packages\n* Structured career paths with opportunities for professional growth\n* Company\\-sponsored employee appreciation events\n* Employee health and wellness initiatives\n\n**Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024\n* Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility\n\n **What to Expect Next**\nA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768198291609","seoName":"clinical-research-physician","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-laboratory-technical-services/clinical-research-physician-6504938132608112/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"289d2ce7-b4d3-49e9-9784-0801d73df08a","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1768198291609,"categoryName":"Laboratory & Technical Services","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4380","location":"C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain","infoId":"6504938130969812","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Pediatric / Neuromuscular Neurologist","content":"Job Summary :\n\nWe are seeking a Pediatric / Neuromuscular Neurologist to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \n\n\\*\\*All Medical Directors have hybrid WFH flexibility.\nResponsibilities :\n* Provide medical management and expertise for clinical trials;\n* Contribute medical expertise to study reports, regulatory documents, and manuscripts;\n* Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;\n* Participate in new business development through involvement in proposal and sponsor meetings as requested;\n* Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;\n* Follow specific research related protocol and lead others in strict adherence to the policies.\n\n\nQualifications :\n* Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred;\n* Prior clinical trial research experience preferred; and\n* Previous experience in pharmaceutical\\-related clinical research is preferred.\n\n\n Travel: up to 20%\nMedpace Overview :\n\nMedpace is a full\\-service clinical contract research organization (CRO). We provide Phase I\\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\\-viral and anti\\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\\+ countries.\nWhy Medpace? :\n\nPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. \n\nThe work we’ve done over the past 30\\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks**\n\n* Flexible work environment\n* Competitive compensation and benefits package\n* Competitive PTO packages\n* Structured career paths with opportunities for professional growth\n* Company\\-sponsored employee appreciation events\n* Employee health and wellness initiatives\n\n**Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024\n* Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility\n\n **What to Expect Next**\nA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768198291481","seoName":"pediatric-neuromuscular-neurologist","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-laboratory-technical-services/pediatric-neuromuscular-neurologist-6504938130969812/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"331f1aab-8e7e-4c5a-8261-f62603d1486d","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1768198291481,"categoryName":"Laboratory & Technical Services","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4380","location":"C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain","infoId":"6504938129254712","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Hepatology - Medical Director","content":"Job Summary :\n\nWe are seeking a Hepatologist to join our team in London. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. \n\n\\*\\*All Medical Monitors have hybrid WFH flexibility.\nResponsibilities :\n* Provide medical management and expertise for clinical trials;\n* Contribute medical expertise to study reports, regulatory documents, and manuscripts;\n* Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;\n* Participate in new business development through involvement in proposal and sponsor meetings as requested;\n* Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;\n* Follow specific research related protocol and lead others in strict adherence to the policies.\n\n\nQualifications :\n* Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred;\n* Prior clinical trial research experience preferred; and\n* Previous experience in pharmaceutical\\-related clinical research is preferred.\n\n\n Travel: up to 20%\nMedpace Overview :\n\nMedpace is a full\\-service clinical contract research organization (CRO). We provide Phase I\\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\\-viral and anti\\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\\+ countries.\nWhy Medpace? :\n\nPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. \n\nThe work we’ve done over the past 30\\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks**\n\n* Flexible work environment\n* Competitive compensation and benefits package\n* Competitive PTO packages\n* Structured career paths with opportunities for professional growth\n* Company\\-sponsored employee appreciation events\n* Employee health and wellness initiatives\n\n**Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024\n* Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility\n\n **What to Expect Next**\nA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768198291347","seoName":"hepatology-medical-director","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-laboratory-technical-services/hepatology-medical-director-6504938129254712/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"79443a49-a6e5-40e1-b7e1-6913fb3c7188","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1768198291347,"categoryName":"Laboratory & Technical Services","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4380","location":"C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain","infoId":"6504938127590712","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Psychiatry - Medical Director","content":"Job Summary :\n\nWe are seeking a Psichiatry Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \n\n\\*\\*All Medical Directors have hybrid WFH flexibility.\nResponsibilities :\n* Provide medical management and expertise for clinical trials;\n* Contribute medical expertise to study reports, regulatory documents, and manuscripts;\n* Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;\n* Participate in new business development through involvement in proposal and sponsor meetings as requested;\n* Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;\n* Follow specific research related protocol and lead others in strict adherence to the policies.\n\n\nQualifications :\n* Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred;\n* Prior clinical trial research experience preferred; and\n* Previous experience in pharmaceutical\\-related clinical research is preferred.\n\n\n Travel: up to 20%\nMedpace Overview :\n\nMedpace is a full\\-service clinical contract research organization (CRO). We provide Phase I\\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\\-viral and anti\\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\\+ countries.\nWhy Medpace? :\n\nPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. \n\nThe work we’ve done over the past 30\\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks**\n\n* Flexible work environment\n* Competitive compensation and benefits package\n* Competitive PTO packages\n* Structured career paths with opportunities for professional growth\n* Company\\-sponsored employee appreciation events\n* Employee health and wellness initiatives\n\n**Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024\n* Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility\n\n **What to Expect Next**\nA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1768198291218","seoName":"psychiatry-medical-director","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-laboratory-technical-services/psychiatry-medical-director-6504938127590712/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"f55237db-5815-4aa5-bca9-ea8cedf0271f","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1768198291218,"categoryName":"Laboratory & Technical Services","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4380","location":"C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain","infoId":"6504938125913712","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Dermatologist - Medical Director","content":"Job Summary :\n\nWe are seeking an Dermatologist \\- Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \n\n\\*\\*All Medical Directors have hybrid WFH flexibility.\nResponsibilities :\n* Provide medical management and expertise for clinical trials;\n* Contribute medical expertise to study reports, regulatory documents, and manuscripts;\n* Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;\n* Participate in new business development through involvement in proposal and sponsor meetings as requested;\n* Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;\n* Follow specific research related protocol and lead others in strict adherence to the policies.\n\n\nQualifications :\n* Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred;\n* Prior clinical trial research experience preferred; and\n* Previous experience in pharmaceutical\\-related clinical research is preferred.\n\n\n Travel: up to 20%\nMedpace Overview :\n\nMedpace is a full\\-service clinical contract research organization (CRO). We provide Phase I\\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\\-viral and anti\\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\\+ countries.\nWhy Medpace? :\n\nPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. \n\nThe work we’ve done over the past 30\\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. 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Reino Unido, 7, 28880 Meco, Madrid, Spain","infoId":"6504937018547512","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Personal warehouse laboratory","content":"Warehouse assistant sought for a major pharmaceutical laboratory in Meco. The position focuses on the distribution area, where the candidate will actively participate in organizing and ensuring the smooth operation of the warehouse.\n \n \n\nMain responsibilities include ensuring compliance with the laboratory's quality standards, as well as performing cleaning and maintenance tasks for the facility. 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This internship is tailored for ambitious individuals seeking real\\-world exposure in financial modeling, transaction analysis, and strategic advisory. 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Para nosotros, el progreso es el estándar —para ti, tu equipo y todo el mundo. Como líder global, te brindamos lo que necesitas para lograrlo. No siempre será fácil; el desarrollo exige determinación. Pero en ABB nunca actuarás solo. Gestiona aquello que impulsa al mundo.\n\n\nEste puesto depende de:\n\n\nChapter Lead (Piloto ELSP) \n\nComo Analista Funcional de Negocio, formarás parte de la Unidad Ágil de Procesos y Herramientas Comerciales para la Habilitación Empresarial, dentro del Capítulo de Análisis Funcional de Comercio Electrónico. Trabajarás en el Equipo Ágil «Gestionar el Marco de Colaboración y Compartición de Conocimiento», cuya misión es gestionar el marco de colaboración de la División para apoyar la planificación, la generación de ideas y la compartición de conocimientos sobre diseños estándar, mejores prácticas y directrices.\n\n\nTendrás la oportunidad de ser responsable del análisis, gestión, desarrollo y mejora de procesos comerciales globales e integrados de extremo a extremo. Al colaborar con los interesados del negocio y de Sistemas de Información (IS), serás responsable de cerrar la brecha entre el entorno empresarial y el técnico, recopilando requisitos comerciales y utilizando el análisis de datos para evaluar procesos y definir desafíos, oportunidades y soluciones, con el fin de respaldar las decisiones relativas a nuevas soluciones o servicios de IS, o a su mejora.\n\n\nEste puesto contribuye a nivel mundial a **Electrificación Inteligente de Energía**.\n\n\nUbicación preferida: Europa\n\n\nEl modelo de trabajo para este puesto es: Híbrido\n\n**Serás principalmente responsable de:**\n\n* Identificar, recopilar, analizar y priorizar los requisitos comerciales, traduciéndolos hábilmente en historias de implementación para el desarrollo de herramientas destinadas a la Planificación Estratégica y de Cartera, la Ejecución y Entrega del Backlog, así como herramientas y plataformas de tickets para la compartición de conocimiento\n* Traducir los requisitos comerciales en especificaciones para equipos de desarrollo internos y externos\n* Colaborar estrechamente con los usuarios finales y el equipo de desarrollo para establecer planes de desarrollo claros y criterios de aceptación verificables, garantizando una alineación perfecta y aprovechando las mejores prácticas para cumplir los requisitos comerciales\n* Brindar análisis específicos para funciones comerciales, aportando experiencia técnica y en procesos comerciales/datos para respaldar las decisiones relativas a nuevas soluciones o servicios de IS, o a sus modificaciones\n* Trabajar junto con desarrolladores y el área de IS para estimar y supervisar el esfuerzo de desarrollo, incluyendo capacidad, estado y velocidad, en todos los desarrollos y lanzamientos planificados\n* Confirmar si la solución entregada cumple con la especificación real durante las Pruebas de Aceptación por el Usuario\n* Brindar capacitación y orientación a los usuarios de las herramientas\n* Informar y actualizar a los principales interesados sobre el avance del proyecto\n\n**Requisitos del puesto:**\n\n* Título universitario en Ingeniería, Ciencias de la Computación, Matemáticas, Física o Estadística\n* 3+ años de experiencia en puestos técnicos o de liderazgo similares\n* Competencia técnica en Salesforce y herramientas impulsadas por IA; habilidades en Python (programación orientada a objetos) y conocimientos prácticos de Docker, GitLab CI/CD, Azure DevOps, Jira y Linux\n* Amplios conocimientos de metodologías ágiles, ofreciendo liderazgo y orientación a los equipos en la gestión del backlog y la entrega\n* Excelentes capacidades analíticas y de gestión de riesgos, con una sólida comprensión financiera para estimar costos, esfuerzos y gestionar la demanda de soluciones de IS\n* Conocimiento de tecnologías de IA y su aplicación para optimizar procesos comerciales y la toma de decisiones\n* Dominio fluido del inglés, con excelentes habilidades comunicativas y de gestión de interesados\n\n**¿Qué obtienes tú?**\n\n\nTe empoderamos para asumir la iniciativa, compartir ideas audaces y dar forma a resultados reales. Crecerás mediante experiencia práctica, tutoría y aprendizaje adaptado a tus objetivos. Aquí, tu trabajo no solo importa: impulsa el progreso.\n\n**Más sobre nosotros**\n\n\nABB Smart Power ofrece soluciones de distribución energética para centros de datos, plantas industriales y de fabricación, infraestructuras críticas y edificios comerciales. Los equipos técnicos de la División trabajan en estrecha colaboración con socios industriales, entregando soluciones avanzadas que apoyan un crecimiento acelerado, la transición energética y los objetivos de sostenibilidad. El portafolio de la División incluye interruptores automáticos industriales, sistemas de baja tensión, aplicaciones de arranque de motores y dispositivos de seguridad como interruptores y relés. Su unidad Power Protection brinda a las mayores empresas mundiales de centros de datos soluciones avanzadas de UPS eficientes desde el punto de vista energético. El ABB Ability™ Energy Manager de la División ofrece una plataforma escalable y fácil de usar que ayuda a las organizaciones a ahorrar energía y reducir sus emisiones de CO2.\n\n**Llamado a la acción**\n\n\nGuía el futuro. Aquí es donde la innovación se acelera, las industrias se reinventan y tu impacto impulsa al mundo hacia adelante. Run What Runs the World.\n\n\n#ABBCareers\n\n\n#RunwithABB\n\n\n#Runwhatrunstheworld\n\n\n#Agile\n\n\n#Electrification\n\n\n#SmartPower\n\n\n#FunctionalAnalyst\n\n\n#BusinessDeveloper\n\n\nValoramos la diversidad de experiencias. ¿Podría ser esta tu historia? ¡Postúlate ya o visita www.abb.com para conocer más sobre nosotros y descubrir el impacto de nuestras soluciones en todo el mundo.","price":"","unit":"per year","currency":null,"company":"Indeed","language":"en","online":1,"infoType":1,"biz":"jobs","postDate":"1767587318000","seoName":"ecommerce-functional-analyst","supplement":null,"author":null,"originalPrice":null,"soldCnt":null,"topSeller":null,"source":1,"cardType":null,"action":"https://es.ok.com/en/city-yebes/cate-math-stats-info-sciences/ecommerce-functional-analyst-6497117682969912/","localIds":null,"cateId":null,"tid":null,"logParams":{"tid":"65fa18ff-214f-4145-ad24-ab5fa4ea7bb2","sid":"7cffac6f-4f03-4079-9be0-e1ea075a9cc0"},"attrParams":{"summary":null,"employment":[{"icon":"https://sgj1.ok.com/yongjia/bkimg/8hvituaa__w72_h72.webp","name":"Job Type","value":"Full-time","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/is8j0f44__w72_h72.webp","name":"Workplace type","value":"Onsite","unit":null},{"icon":"https://sgj1.ok.com/yongjia/bkimg/ji66qqr0__w72_h72.webp","name":null,"value":"Madrid,Comunidad de Madrid","unit":null}]},"addDate":1767587318981,"categoryName":"Mathematics · Statistics & Information Sciences","postCode":null,"secondCateCode":"science-technology","kycTag":null,"pictureUrls":null,"priceDetail":null,"featureLabels":null,"supplementList":null,"soldCntStr":null,"companyLogo":null,"reportStatus":null,"isFavorite":false},{"category":"4000,4374,4380","location":"6MPX+8P Tielmes, Spain","infoId":"6496090520653012","pictureUrl":"https://uspic3.ok.com/logo/ineed.png","videos":null,"title":"Quality Control Technician","content":"We are looking for a Quality Control Technician to join our team in Tielmes de Tajuña. 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The team works hand\\-on\\-hand with Statisticians, Epidemiologists and disease area experts across the wider global Real\\-World Solutions group, leveraging a vast variety of anonymous patient\\-level information. The data encompasses IQVIA’s access to over 530 million anonymised patients as well as bespoke, custom partnerships with healthcare providers and payers.\n**Why Join?**Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. In IQVIA, you will have access to the most cutting\\-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry.\n**We thank all applicants for their interest; however, only those selected for an interview will be contacted**\nIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. 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